24 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES HIGH TIBIAL OSTEOTOMY PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450806319·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571071·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571040·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571088·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571095·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571057·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571033·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571064·
NA
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·March 7, 2012
DERMACLEAR UV-B PHOTOTHERAPY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EXEL SECURE TOUCH SAFETY (P.S.V.) SCALP VEIN SET
FDA 510(k)
FDA Class 2
·General Hospital
TRACHEOSTOMY TUBE
FDA Adverse Event
Injury
·KENDALL GAMMATRON, THAILAND·Product code BTR·September 8, 2019
VERTE-STACK K030736, K041197
FDA Adverse Event
Death
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·January 4, 2019
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·March 14, 2014
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·March 15, 2014
URETEX SUPPORT PP TRANSOBTUR2 KIT X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTN·March 12, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 13, 2008
BD ULTRA FINE PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·August 17, 2020